Devices and methods for long-term intracellular access

Patent metadata

Field	Value
Publication number	US-9856448-B2
Application number	US-201414461303-A
Country	US
Kind code	B2
Filing date	Aug 15, 2014
Priority date	Mar 4, 2011
Publication date	Jan 2, 2018
Grant date	Jan 2, 2018

Abstract

Nanoscale probes for forming stable, non-destructive seals with cell membranes. The probes, systems including these probes, and methods of fabricating and using the probes described herein may be used to sense from, stimulate, modify, or otherwise effect individual cells or groups of cells. In particular, described herein are nanoscale cellular probes that may be used to fuse with, and in some variations span, the lipid membrane of a cell to provide stable and long lasting contact to the cell. Thus, the probes described herein may be used as part of a system, method or device that would benefit from stable, non-destructive access to and across a cell membrane. In some variations the nanoscale probe devices or systems described herein may be used as part of a drug screening procedure.

First claim

What is claimed is:

1. A probe for sealing with a cell membrane, the probe comprising:
a base region extending in a horizontal plane;
a hollow elongate member projecting distally up from the base region, the hollow elongate member having a distal end with a diameter of between about 200 nm and 5 μm and a height of between about 10 nm to 5 μm; and
a distal heterofunctional region at the distal end of the hollow elongate member, the distal heterofunctional region extending less than 100 nm from the distal end, wherein the distal heterofunctional region is configured to form a region that is more hydrophobic than the base and a region of the hollow elongate member proximal to the distal heterofunctional region.

2. The probe of claim 1 , wherein the distal end comprises a distal opening into an inner lumen and a wall thickness at the distal opening of between about 0.1 nm and 5 nm.

3. The probe of claim 1 , wherein the distal end comprises a distal opening into an inner lumen, and further comprising an electrode recessed within the inner lumen.

4. The probe of claim 1 , wherein an outer surface of the portion of the hollow elongate member proximal to the distal heterofunctional region is formed of the same material as the base region.

5. The probe of claim 1 , further comprising an electrical contact on the base.

6. The probe of claim 1 , wherein the hollow elongate member comprises a conical shape.

7. The probe of claim 1 , wherein the hollow elongate member has a circular or oval cross-section.

8. The probe of claim 1 , wherein the hollow elongate member has a triangular, rectangular or square cross-section.

9. The probe of claim 1 , wherein the distal heterofunctional region forms a ring at the distal end of the hollow elongate member.

10. The probe of claim 1 , wherein the distal heterofunctional region has a width of between about 5 nm and about 10 nm.

11. The probe of claim 1 , wherein the distal heterofunctional region comprises one or more materials forming a hydrophobic ring at the distal end of the hollow elongate member.

12. The probe of claim 1 , further comprising an inner functionalized region within a recess of the hollow elongate member, comprising an activity marker configured to indicate a cellular state or activity.

13. A probe for sealing with a cell membrane, the probe comprising:
a base region extending in a horizontal plane;
a hollow elongate member projecting distally up from the base region, the hollow elongate member having a distal opening into an inner lumen, an outer diameter of the distal opening between about 200 nm and 5 μm and a height of between about 10 nm to 5 μm, wherein the hollow elongate member has a wall thickness at the distal opening of between about 0.1 nm and 5 nm;
a distal heterofunctional ring at the distal end of the hollow elongate member, the distal heterofunctional ring extending proximally less than 100 nm from the distal end, wherein the distal heterofunctional ring is configured to form a region that is more hydrophobic than the base and a region of the hollow elongate member proximal to the distal heterofunctional ring; and
an electrode recessed with the inner lumen of the hollow elongate member.

14. The probe of claim 13 , wherein the portion of the hollow elongate member proximal to the distal heterofunctional ring is formed of the same material as the base region.

15. The probe of claim 13 , further comprising an electrical contact on the base.

16. The probe of claim 13 , wherein the hollow elongate member comprises a conical shape.

17. The probe of claim 13 , wherein the hollow elongate member has a circular or oval cross-section.

18. The probe of claim 13 , wherein the hollow elongate member has a triangular, rectangular or square cross-section.

19. The probe of claim 13 , wherein the distal heterofunctional ring forms a ring on an outer surface of the distal end of the hollow elongate member.

20. The probe of claim 13 , wherein the distal heterofunctional ring has a width of between about 5 and about 10 nm.

21. The probe of claim 13 , wherein the distal heterofunctional ring comprises one or more materials forming a hydrophobic ring at the distal end of the hollow elongate member.

22. The probe of claim 13 , further comprising an inner functionalized region within a recess of the hollow elongate member, comprising an activity marker configured to indicate a cellular state or activity.

23. A probe for sealing with a cell membrane, the probe comprising:
a base region extending in a horizontal plane;
a hollow elongate member projecting distally up from the base region, the hollow elongate member having a distal opening into an inner lumen, an outer diameter of the distal opening between about 200 nm and 5 μm and a height of between about 10 nm to 5 μm wherein the hollow elongate member has a wall thickness at the distal opening of between about 0.1 nm and 5 nm; and
a distal heterofunctional ring at the distal end of the hollow elongate member, the distal heterofunctional ring extending less than 100 nm from the distal end of the hollow elongate member, wherein the distal heterofunctional ring comprises a cell-adhesion motif and is configured to fuse to a cell membrane.

24. The probe of claim 23 , wherein the distal heterofunctional ring comprises a cell-adhesion motif from the group consisting of: cell surface receptors, polylysine, polyornithine, fibronectin, Arginylglycylaspartic acid (RGD) and integrins.

25. A method of sealing onto and measuring a parameter from a cell, the method comprising:
contacting a cell membrane of a cell with a probe comprising a hollow elongate member projecting distally up from the base region between about 10 nm to 5 μm, the hollow elongate member having a distal opening into an inner lumen, an outer diameter of the distal opening between about 200 nm and 5 μm, wherein the hollow elongate member has a wall thickness at the distal opening of between about 0.1 nm and 5 nm;
forming a seal with the cell membrane at a distal heterofunctional ring at the distal end of the hollow elongate member, the distal heterofunctional ring extending proximally less than 100 nm from the distal end of the hollow elongate member.

26. The method of claim 25 , wherein the distal heterofunctional ring forms a region that is more hydrophobic than the base and a region of the hollow elongate member proximal to the distal heterofunctional ring.

27. The method of claim 25 , wherein the distal heterofunctional ring comprises a cell-adhesion motif.

28. The method of claim 25 , wherein the distal heterofunctional ring comprises a cell-adhesion motif from the group consisting of: cell surface receptors, polylysine, polyornithine, fibronectin, Arginylglycylaspartic acid (RGD) and integrins.

29. The method of claim 25 , wherein forming a seal comprises fusing the distal heterofunctinoal ring with the cell membrane.

30. The method of claim 25 , further comprising recording a cellular state or activity using an electrode within a recess in the inner lumen of the hollow elongate member.

Assignees

• Univ Leland Stanford Junior
• The Board Of Trustees Of The Leland Stanford Junior Univesity

Inventors

• Melosh Nicholas Alexander
• Verma Piyush
• Almquist Benjamin David

Classifications

• C12M35/00 Primary

  Means for application of stress for stimulating the growth of microorganisms or the generation of fermentation or metabolic products; Means for electroporation or cell fusion (machines for extracting juice from animal or plant tissue by electroplasmolysis A23N1/006, processes employing electric or wave energy B01J19/08; treatment of microorganisms or enzymes with electrical or wave energy C12N13/00; methods for cell fusion C12N15/02; introduction of foreign genetic material C12N15/87) · CPC title

• G01N33/48728

  Investigating individual cells, e.g. by patch clamp, voltage clamp (investigating individual particles in general G01N15/10) · CPC title